WO1994006269A1 - Procede de (co)polymerisation de monomeres vinyliques - Google Patents

Procede de (co)polymerisation de monomeres vinyliques Download PDF

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Publication number
WO1994006269A1
WO1994006269A1 PCT/EP1993/002426 EP9302426W WO9406269A1 WO 1994006269 A1 WO1994006269 A1 WO 1994006269A1 EP 9302426 W EP9302426 W EP 9302426W WO 9406269 A1 WO9406269 A1 WO 9406269A1
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WO
WIPO (PCT)
Prior art keywords
peroxy
methylpentyl
radical polymerization
polymerization initiator
weight
Prior art date
Application number
PCT/EP1993/002426
Other languages
English (en)
Inventor
Takumi Fukumura
John Meijer
Original Assignee
Kayaku Akzo Corporation
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Kayaku Akzo Corporation filed Critical Kayaku Akzo Corporation
Priority to EP93919297A priority Critical patent/EP0659194B1/fr
Priority to DE69305358T priority patent/DE69305358T2/de
Priority to US08/397,102 priority patent/US5674958A/en
Publication of WO1994006269A1 publication Critical patent/WO1994006269A1/fr

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F4/00—Polymerisation catalysts
    • C08F4/28—Oxygen or compounds releasing free oxygen
    • C08F4/32—Organic compounds
    • C08F4/34—Per-compounds with one peroxy-radical

Definitions

  • the present invention relates to a process for (co)polymerizing vinyl monomers in the presence of a radical polymerization initiator.
  • U.S. patents 3,726,847 and 3,624,123 disclose a long list of t- alkylperoxy esters and their precursors, viz. hydroperoxides.
  • the long list of hydroperoxides includes 3-methyl-3-hydroperoxy pentyne-1, which may also be used as a saturated hydroperoxide.
  • These patent publications suggest that t-alkylperoxy esters can be used in the polymerization of vinyl monomers.
  • t-butylperoxy pivalate (TBPP), t-butylperoxy neodecanoate (TX23), and ⁇ -cumylperoxy neodecanoate (CND) are exemplified.
  • 3-methylpentyl-3-peroxy alkanoates are neither exemplified nor preferred.
  • Dutch patent application 69 15160 discloses the use of t-hexylperoxy alkanoate for the polymerization and/or curing of vinyl monomers. No specifics are given on the structure of this t-hexyl compound. However, from U.S. patents 4,057,567 and 4,063,013 it can be concluded that t-hexylperoxy alkanoate is 2-methylpentyl-2-peroxy alkanoate. These patent publications also disclose the use of 2-methylpentyl-2-peroxyalkanoates in the polymerization of vinyl monomers. Exemplified is 2-methylpentyl-2-peroxy neodecanoate (THPND) .
  • THPND 2-methylpentyl-2-peroxy neodecanoate
  • SUBSTITUTE SHEET polymer are satisfactory. It has also been found that the use of THPND results in a low polymer conversion. In addition, CND imparts a peculiar, offensive smell to the polymer due to the presence of decomposition products.
  • the present invention relates to a process for (co)polymerizing vinyl monomers in the presence of a radical polymerization initiator, characterized in that said radical polymerization initiator is a 3-methylpentyl-3-peroxy alkanoate of the formula (I)
  • R ⁇ , R 2 and R3 represent alky! groups each having at most 9 carbon atoms with the proviso that the total number of carbon atoms of R l> R 2 an d R 3 " > s at ost l- > sa" ' c ' 3-methylpentyl-3-peroxy alkanoate being employed in an amount of 0.002 to 2.0 parts by weight, based on 100 parts by weight of monomers present, said process being carried out at a temperature above 20°C.
  • SUBSTITUTE SHEET The use of 3-methylpentyl-3-peroxy alkanoates in the present invention surprisingly and unexpectedly results in a higher polymerization velocity, a shortened polymerization time, and an increase in conversion as compared with the results obtained by using other radical polymerization inititators. It has also been found that the obtained polymer has excellent thermal stability and is not affected by odour or colouration. Thus the industrial value of the radical polymerization initiator of the present invention is remarkably high.
  • 3-methylpentyl-3-peroxy alkanoate of the formula (I) to be used in the present invention examples include 3-methylpentyl-3-peroxy pivalate (3MPPP), 3-methylpentyl-3-peroxy neohexanoate, 3-methylpentyl-3-peroxy neoheptanoate, 3-methylpentyl-3-peroxy neooctanoate, 3-methylpentyl-3-peroxy neononanoate, 3-methylpentyl-3-peroxy neodecanoate (3MPPND) and 3-methylpentyl-3-peroxy neotridecanoate.
  • 3MPPP 3-methylpentyl-3-peroxy pivalate
  • 3-methylpentyl-3-peroxy neohexanoate 3-methylpentyl-3-peroxy neoheptanoate
  • 3-methylpentyl-3-peroxy neooctanoate 3-methylpentyl-3
  • 3-Methylpentyl-3-peroxy alkanoates are known compounds. They are, for example, disclosed by Yurzhenko, T.I., et al., Zh. Org. Khim. 3(9), 1705-6 (1967). This publication, however, does not reveal any industrial application of the compounds.
  • the radical polymerization initiators used in the present invention can be produced in a high yield under reaction conditions similar to those of conventional processes. More specifically, the peroxide may be produced by reacting a carboxylic acid chloride with 3-methylpentyl-3-hydroperoxide in the presence of potassium hydroxide, sodium hydroxide or mixtures thereof at a temperature in the range of 0° to 30°C.
  • carboxylic acids to be used as the starting material for the above-described carboxylic acid chloride include pivalic acid, neohexanoic acid, neoheptanoic acid, neooctanoic acid, neononanoic
  • SUBSTITUTE SHEET acid (such as Equacid ® 9, ex Idemitsu Petrochemical Co., Ltd.), neodecanoic acid and neotridecanoic acid (such as Equacid ® 13, ex Idemitsu Petrochemical Co., Ltd.).
  • the 3-methylpentyl-3-peroxy alkanoates to be used in the present invention may be prepared in the form of a solution by adding an isoparaffinic aliphatic hydrocarbon (such as IP-1620 Solvent, ex Idemitsu Petrochemical Co., Ltd.) to the reaction system, or a pure 3-methylpentyl 3-peroxy alkanoate may be synthesized and later diluted with a solvent.
  • an isoparaffinic aliphatic hydrocarbon such as IP-1620 Solvent, ex Idemitsu Petrochemical Co., Ltd.
  • radical polymerization initiator of the formula (I) may be used in the present invention in combination with other radical polymerization initiators in order to attain a uniform polymerization velocity.
  • radical polymerization initiators include peroxy dicarbonates such as diisopropylperoxy dicarbonate (IPP), di (2-ethylhexyl)peroxy dicarbonate (EHP), and di (sec-butyl)peroxy dicarbonate (SBP); peroxy esters such as t-butylperoxy pivalate (TBPP), t-butylperoxy neodecanoate (TX23), and ⁇ -cumylperoxy neodecanoate (CND); diacyl peroxides such as diisobutyryl peroxide (IB), dilauroyl peroxide (LP), and bis-3,5,5-trimethylhexanoyl peroxide (TX36); peroxides such as acetyl cyclohexylsulfonyl peroxide (ACSP); and azo compounds such as azobisisobutyronitrile (AIBN).
  • IPP diisopropylperoxy dicarbonate
  • Examples of the monomers usable in the process of the present invention include vinyl chloride, vinylidene chloride, vinyl acetate, and methyl methacrylate, and mixtures thereof, as well as other monomers copolymerizable there with, such as ethylene, propylene, styrene, acrylic acid, acrylic ester, ethacrylic acid, and methacrylic ester.
  • polymerization is conducted by any conventional process, except that a specified radical polymerization initiator is used.
  • the amount of the radical polymerization initiator which varies depending on the polymerization temperature, the capacity for removing the heat of polymerization, and, when applicable, the kind of comonomer to be used, is usually 0.002 to 2.0 parts by weight, preferably 0.005 to 1.0 parts by weight, based on 100 parts by weight of monomers present.
  • radical polymerization initiator used When the amount of radical polymerization initiator used is below 0.002 parts by weight, the polymerization velocity and conversion are too low, so that the polymerization will not be completed. When the amount of radical polymerization initiator exceeds 2.0 parts by weight, controlling the polymerization velocity becomes difficult and may lead to a runaway polymerization reaction.
  • the amount of other radical polymerization initiator to be used in combination with the radical polymerization initiator of the present invention must be such that the effect of the radical polymerization initiator of the present invention will be not inhibited.
  • the polymerization temperature is usually 20° to 75°C, preferably 30° to 70°C. When it is below 20°C, the polymerization time becomes too long. However, when it exceeds 75°C, the radical polymerization initiator is spent in the initial stage of the polymerization, making it difficult to attain a high conversion. In order to reduce the amount of unreacted monomer, however, it is also possible to conduct polymerization in the temperature range of 20° to 75°C and then elevate the temperature above 75°C (up to about 130°C) to complete the polymerization.
  • the polymerization may be conducted by any of the suspension, solution, emulsion and bulk polymerization processes, but is not limited in any respect other than that the radical polymerization initiator of the above formula (I) is used in the present invention.
  • TX23 t-butylperoxy neodecanoate
  • polymers obtained by the present invention are superior to those obtained by using an ordinary radical polymerization initiator in both hue and odour.
  • the conversion was 97.7%.
  • the weight-average and number-average molecular weights determined by gel permeation chromatography were 497 200 and 159400, respectively.
  • the polymerization process was repeated, except that 3MPPND was replaced with 0.30 parts by weight of 2-methylpentyl-2-peroxy neodecanoate (THPND).
  • THPND 2-methylpentyl-2-peroxy neodecanoate
  • the conversion was 94.3%, while the weight-average molecular weight was 533 900 and the number-average molecular weight was 161 800.
  • a 10% solution of sodium hydroxide in methanol was added to the polyvinyl acetate thus obtained to conduct saponification at 30°C for 3 hours to obtain polyvinyl alcohol.
  • the degree of polymerization of the obtained polyvinyl alcohol was 1740.
  • the polymerization process was repeated except that 3MPPP was replaced with 0.004 parts by weight of 2-methylpentyl-2-peroxy pivalate (THPP) .
  • THPP 2-methylpentyl-2-peroxy pivalate
  • the conversion of vinyl acetate was 69.6% and the degree of polymerization was 2210.
  • the degree of polymerization of the polyvinyl alcohol obtained after saponification was 1790.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polymerization Catalysts (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Polymerisation Methods In General (AREA)

Abstract

L'invention concerne un procédé de (co)polymérisation de monomères vinyliques en présence d'un initiateur de polymérisation radicalaire, caractérisé en ce que ce dernier est un alcanoate de 3-méthylpenthyle-3-peroxy de la formule (I), dans laquelle R1, R2 et R3 représentent des groupes alkyle comportant chacun au plus 9 atomes de carbones, à la condition que le nombre total d'atomes de carbone de R1, R2 et R3 soit au maximum de 11, ledit alcanoate de 3-méthylpenthyle-3-peroxy étant utilisé en une dose comprise entre 0,002 et 2,0 parties en poids, sur la base de 100 parties en poids de monomères présents, ledit procédé étant mis en ÷uvre à une température supérieure à 20 °C. L'utilisation d'alcanoates de 3-méthylpenthyle-3-peroxy dans l'invention a pour résultats surprenants et inattendus une vitesse de polymérisation supérieure, un temps de polymérisation raccourci, ainsi qu'une augmentation de la conversion comparée aux résulats obtenus lors de l'utilisation d'autres initiateurs de polymérisation radicalaires. On a également découvert que le polymère obtenu présente une excellente stabilité thermique et n'est pas affecté par une odeur ou une coloration. Ainsi, la valeur industrielle du peroxyde initiateur de polymérisation radicalaire de l'invention est particulièrement appréciable.
PCT/EP1993/002426 1992-09-08 1993-09-07 Procede de (co)polymerisation de monomeres vinyliques WO1994006269A1 (fr)

Priority Applications (3)

Application Number Priority Date Filing Date Title
EP93919297A EP0659194B1 (fr) 1992-09-08 1993-09-07 Procede de (co)polymerisation de monomeres vinyliques
DE69305358T DE69305358T2 (de) 1992-09-08 1993-09-07 Verfahren zur (co)polymerisation von vinyl-monomeren
US08/397,102 US5674958A (en) 1992-09-08 1993-09-07 Process for (co)polymerizing vinyl monomers

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP264064/1992 1992-09-08
JP26406492A JP3165525B2 (ja) 1992-09-08 1992-09-08 ビニル系単量体の重合方法

Publications (1)

Publication Number Publication Date
WO1994006269A1 true WO1994006269A1 (fr) 1994-03-17

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Application Number Title Priority Date Filing Date
PCT/EP1993/002426 WO1994006269A1 (fr) 1992-09-08 1993-09-07 Procede de (co)polymerisation de monomeres vinyliques

Country Status (8)

Country Link
US (1) US5674958A (fr)
EP (1) EP0659194B1 (fr)
JP (1) JP3165525B2 (fr)
AT (1) ATE143979T1 (fr)
CA (1) CA2143958A1 (fr)
DE (1) DE69305358T2 (fr)
ES (1) ES2095668T3 (fr)
WO (1) WO1994006269A1 (fr)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010126041A1 (fr) * 2009-04-28 2010-11-04 日本合成化学工業株式会社 Composition de résine d'alcool polyvinylique
JP5641769B2 (ja) * 2009-04-28 2014-12-17 日本合成化学工業株式会社 水溶性ポリビニルアルコール系樹脂組成物
KR200480424Y1 (ko) * 2014-09-17 2016-05-24 (주)제이엔디 주차 표시등 장치

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1550289A (fr) * 1966-11-09 1968-12-20
NL6915160A (fr) * 1968-10-07 1970-04-09
US4063013A (en) * 1973-02-20 1977-12-13 Argus Chemical Corporation T-Alkyl peresters of t-hydroperoxides catalysts for polymerization of unsaturated monomers
JPH01104605A (ja) * 1987-10-19 1989-04-21 Chisso Corp 塩化ビニル系重合体の製造方法
WO1991003496A1 (fr) * 1989-09-01 1991-03-21 Gaf Chemicals Corporation Procede de polymerisation a l'aide de pivalate tertiaire-amylperoxy comme initiateur du radical libre

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1104605A (en) * 1966-05-06 1968-02-28 Von Roll Ag A process and an apparatus for the combustion of solid wastes
US3726847A (en) * 1968-05-01 1973-04-10 Argus Chem Polymerization method employing t-alkyl peresters of t-hydroperoxides
US4057567A (en) * 1968-05-01 1977-11-08 Argus Chemical Corporation Polymerization method and t-alkyl peresters of t-hydroperoxides for use therein
US3624123A (en) * 1968-05-01 1971-11-30 Argus Chem t-ALKYL PERESTERS OF t-HYDROPEROXIDES
JP2567726B2 (ja) * 1990-09-04 1996-12-25 三菱レイヨン株式会社 メタクリル樹脂板の製造方法

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1550289A (fr) * 1966-11-09 1968-12-20
NL6915160A (fr) * 1968-10-07 1970-04-09
DE1950536A1 (de) * 1968-10-07 1970-04-23 Nippon Oils & Fats Co Ltd Peroxyester von tertiaeren Fettsaeuren
US4063013A (en) * 1973-02-20 1977-12-13 Argus Chemical Corporation T-Alkyl peresters of t-hydroperoxides catalysts for polymerization of unsaturated monomers
JPH01104605A (ja) * 1987-10-19 1989-04-21 Chisso Corp 塩化ビニル系重合体の製造方法
WO1991003496A1 (fr) * 1989-09-01 1991-03-21 Gaf Chemicals Corporation Procede de polymerisation a l'aide de pivalate tertiaire-amylperoxy comme initiateur du radical libre

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
DATABASE WPI Week 8922, Derwent World Patents Index; AN 89-161872 *

Also Published As

Publication number Publication date
CA2143958A1 (fr) 1994-03-17
JPH0687909A (ja) 1994-03-29
ATE143979T1 (de) 1996-10-15
DE69305358T2 (de) 1997-03-06
EP0659194B1 (fr) 1996-10-09
US5674958A (en) 1997-10-07
EP0659194A1 (fr) 1995-06-28
DE69305358D1 (de) 1996-11-14
JP3165525B2 (ja) 2001-05-14
ES2095668T3 (es) 1997-02-16

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